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Electrochemical copper dissolution: A benchmark for stable CO2 reduction on copper electrocatalysts

[Display omitted] •Time and potential resolved dissolution of copper at CO2RR relevant pH.•Quantification of Cu electrochemical dissolution using ICP–MS.•Guideline for academic accelerated stress testing of copper based CO2RR catalysts.•Guideline for stable operational conditions of CO2RR electrolys...

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Bibliographic Details
Published in:Electrochemistry communications 2020-06, Vol.115, p.106739, Article 106739
Main Authors: Speck, Florian D., Cherevko, Serhiy
Format: Article
Language:English
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Summary:[Display omitted] •Time and potential resolved dissolution of copper at CO2RR relevant pH.•Quantification of Cu electrochemical dissolution using ICP–MS.•Guideline for academic accelerated stress testing of copper based CO2RR catalysts.•Guideline for stable operational conditions of CO2RR electrolysers. Copper is well known in fundamental electrocatalysis research due to its ability to selectively reduce CO2 to C2 products. Recent, more applied studies have revealed that electrolyzers based on Cu electrocatalysts can reach current densities of up to hundreds of mA cm−2. This opens up the opportunity for industrial application of Cu-based electrocatalysts. However, the stability of copper must first be assessed. In this communication we investigate the electrochemical corrosion behavior of copper in a broad pH window relevant to CO2 reduction applications. Using an electrochemical on-line inductively coupled plasma mass spectrometer (ICP-MS), we quantify Cu dissolution during anodic oxidation and during the reduction of electrochemically formed oxide species. We show that electrochemical oxidation of Cu leads to high dissolution in neutral and highly alkaline environments, while an intermediate pH of around 9–10 leads to minimal dissolution. The obtained results are discussed in relation to the CO2 reduction reaction to set a benchmark for stable Cu-based electrocatalysts.
ISSN:1388-2481
1873-1902
DOI:10.1016/j.elecom.2020.106739